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rs786202200(A;A)

From SNPedia
common genotype
Is agenotype
ofrs786202200
GeneSDHC
Chromosome1
Position161,328,395
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 0 common genotype
(A;G) 6.2 Hereditary PGL/PCC Syndrome
(G;G) 0 common in clinvar
(G;T) 6.2 Hereditary PGL/PCC Syndrome